Cognitive interviewing of the US National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

[1] Trotti A(2003)CTCAE v3.0: Development of a comprehensive grading system for the adverse events of cancer treatment Seminars in Radiation Oncology 13 176-181

[2] Colevas AD(2010)The missing voice of patients in drug-safety reporting New England Journal of Medicine 362 865-869

[3] Setser A(2006)Patient versus clinician symptom reporting using the National Cancer Institute Common Terminology Criteria for Adverse Events: Results of a questionnaire-based study Lancet Oncology 7 903-909

[4] Rusch V(2009)Adverse symptom event reporting by patients versus clinicians: Relationships with clinical outcomes Journal of the National Cancer Institute 101 1624-1632

[5] Jaques D(2012)Reliability of adverse symptom event reporting by clinicians Quality of Life Research 21 1159-1164

[6] Budach V(2012)Comparison between patient-reported and clinician-observed symptoms in oncology Cancer Nursing 19 1421-1427

[7] Basch E(2011)Toxicity and quality of life outcomes in ovarian cancer patients participating in randomized controlled trials Supportive Care in Cancer 5 119-124

[8] Basch E(2012)Patient-reported outcomes versus clinician symptom reporting during chemoradiation for rectal cancer Gastrointestinal Cancer Research 25 5374-5380

[9] Iasonos A(2007)Long-term toxicity monitoring via electronic patient-reported outcomes in patients receiving chemotherapy Journal of Clinical Oncology 14 108-112

[10] McDonough T(2013)Capturing acute toxicity data during lung radiotherapy by using a patient-reported assessment tool Clinical Lung Cancer 105 S74-S81

[1] Trotti A(2003)CTCAE v3.0: Development of a comprehensive grading system for the adverse events of cancer treatment Seminars in Radiation Oncology 13 176-181

[2] Colevas AD(2010)The missing voice of patients in drug-safety reporting New England Journal of Medicine 362 865-869

[3] Setser A(2006)Patient versus clinician symptom reporting using the National Cancer Institute Common Terminology Criteria for Adverse Events: Results of a questionnaire-based study Lancet Oncology 7 903-909

[4] Rusch V(2009)Adverse symptom event reporting by patients versus clinicians: Relationships with clinical outcomes Journal of the National Cancer Institute 101 1624-1632

[5] Jaques D(2012)Reliability of adverse symptom event reporting by clinicians Quality of Life Research 21 1159-1164

[6] Budach V(2012)Comparison between patient-reported and clinician-observed symptoms in oncology Cancer Nursing 19 1421-1427

[7] Basch E(2011)Toxicity and quality of life outcomes in ovarian cancer patients participating in randomized controlled trials Supportive Care in Cancer 5 119-124

[8] Basch E(2012)Patient-reported outcomes versus clinician symptom reporting during chemoradiation for rectal cancer Gastrointestinal Cancer Research 25 5374-5380

[9] Iasonos A(2007)Long-term toxicity monitoring via electronic patient-reported outcomes in patients receiving chemotherapy Journal of Clinical Oncology 14 108-112

[10] McDonough T(2013)Capturing acute toxicity data during lung radiotherapy by using a patient-reported assessment tool Clinical Lung Cancer 105 S74-S81